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Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy

โœ Scribed by Denise D. Belsham; Woon-Chee Yee; Cheryl R. Greenberg; Klaus Wrogemann


Book ID
118931468
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
702 KB
Volume
112
Category
Article
ISSN
0022-510X

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Expansion of trinucleotide repeats has now been associated with eight inherited diseases: X-linked spinal and bulbar muscular atrophy, two fragile X syndromes, myotonic dystrophy, Huntington's disease, spinocerebellar ataxia type I, dentatorubral pallidoluysian atrophy and Machado-Joseph disease. It